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Dover

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Dover FDA UDI
Generic Name
Indwelling urethral catheterization kit, adult FDA UDI
Device Name
Urine Drainage Bag,Needle Sampling, Anti-Reflux Device, Drain Tube FDA UDI
Model / Reference
6261 FDA UDI
Description
Urine Drainage Bag,Needle Sampling, Anti-Reflux Device, Drain Tube FDA UDI

Identifiers

Catalog Number
6261 FDA UDI
Primary DI / UDI-DI
10884521002029 FDA UDI
FDA Product Code
KNX FDA UDI
GMDN Term
Indwelling urethral catheterization kit, adult FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5250 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 4000 Milliliter FDA UDI

Category: Indwelling urethral catheterization kit, adult

Dover by Cardinalhealth — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Indwelling urethral catheterization kit, adult.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 490cf067-203e-4508-95cd-fb059773dc05 37 fields · synced May 31, 2026